NDC 82709-001 Innoble Onechewtoothpaste
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 82709 - Livmate
- 82709-001 - Innoble Onechewtoothpaste
Product Characteristics
Product Packages
NDC Code 82709-001-01
Package Description: 84 g in 1 POUCH
NDC Code 82709-001-03
Package Description: 1 BOTTLE, GLASS in 1 CARTON / 42 g in 1 BOTTLE, GLASS (82709-001-02)
Product Details
What is NDC 82709-001?
What are the uses for Innoble Onechewtoothpaste?
Which are Innoble Onechewtoothpaste UNII Codes?
The UNII codes for the active ingredients in this product are:
- SODIUM FLUORIDE (UNII: 8ZYQ1474W7)
- FLUORIDE ION (UNII: Q80VPU408O) (Active Moiety)
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4) (Active Moiety)
- SODIUM PYROPHOSPHATE (UNII: O352864B8Z)
- PYROPHOSPHORIC ACID (UNII: 4E862E7GRQ) (Active Moiety)
- PYRIDOXINE HYDROCHLORIDE (UNII: 68Y4CF58BV)
- PYRIDOXINE (UNII: KV2JZ1BI6Z) (Active Moiety)
Which are Innoble Onechewtoothpaste Inactive Ingredients UNII Codes?
The inactive ingredients are all the component of a medicinal product OTHER than the active ingredient(s). The acronym "UNII" stands for “Unique Ingredient Identifier” and is used to identify each inactive ingredient present in a product. The UNII codes for the inactive ingredients in this product are:
- SORBITOL (UNII: 506T60A25R)
- SODIUM COCOYL GLUTAMATE (UNII: BMT4RCZ3HG)
- SODIUM COCOYL ISETHIONATE (UNII: 518XTE8493)
- MICROCRYSTALLINE CELLULOSE (UNII: OP1R32D61U)
- XYLITOL (UNII: VCQ006KQ1E)
- MAGNESIUM STEARATE (UNII: 70097M6I30)
- SODIUM BICARBONATE (UNII: 8MDF5V39QO)
- XANTHAN GUM (UNII: TTV12P4NEE)
- HYDROXYPROPYL CELLULOSE, UNSPECIFIED (UNII: 9XZ8H6N6OH)
- LEVOMENTHOL (UNII: BZ1R15MTK7)
- SODIUM CHLORIDE (UNII: 451W47IQ8X)
- MALIC ACID (UNII: 817L1N4CKP)
- COCONUT OIL (UNII: Q9L0O73W7L)
- ALOE VERA LEAF (UNII: ZY81Z83H0X)
- CARROT (UNII: L56Z1JK48B)
* Please review the disclaimer below.
[5] What is the Labeler Name? - Name of Company corresponding to the labeler code segment of the Product NDC.
[9] What is the Start Marketing Date? - This is the date that the labeler indicates was the start of its marketing of the drug product.
[11] What is the Listing Expiration Date? - This is the date when the listing record will expire if not updated or certified by the product labeler.
[12] What is the NDC Exclude Flag? - This field indicates whether the product has been removed/excluded from the NDC Directory for failure to respond to FDA"s requests for correction to deficient or non-compliant submissions ("Y"), or because the listing certification is expired ("E"), or because the listing data was inactivated by FDA ("I"). Values = "Y", "N", "E", or "I".